Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Feingold syndrome
Feingold syndrome type 2
Feingold syndrome type 2 (FS2) is a rare inherited malformation syndrome characterized by skeletal abnormalities and mild intellectual disabilities similar to those seen in Feingold syndrome type 1 (FS1) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures.
This condition has no sub-types.